Use of molecular markers for predicting therapy response in cancer patients

被引:75
作者
Duffy, Michael J. [1 ,2 ,3 ]
O'Donovan, Norma [4 ]
Crown, John [5 ]
机构
[1] St Vincents Univ Hosp, Dept Pathol, Dublin 4, Ireland
[2] St Vincents Univ Hosp, Lab Med, Dublin 4, Ireland
[3] Univ Coll Dublin, Conway Inst Biomol & Biomed Res, UCD Sch Med & Med Sci, Dublin 4, Ireland
[4] Dublin City Univ, Natl Inst Cellular Biotechnol, Dublin 9, Ireland
[5] St Vincents Univ Hosp, Dept Med Oncol, Dublin 4, Ireland
基金
爱尔兰科学基金会;
关键词
Personalized treatment; Cancer; Tumor markers; Biomarkers; Predictive markers; GROWTH-FACTOR-RECEPTOR; TYROSINE KINASE INHIBITORS; METASTATIC BREAST-CANCER; CELL LUNG-CANCER; 21-GENE RECURRENCE SCORE; TOPOISOMERASE-II-ALPHA; PROGESTERONE-RECEPTOR; ESTROGEN-RECEPTOR; MONOCLONAL-ANTIBODY; ADJUVANT TAMOXIFEN;
D O I
10.1016/j.ctrv.2010.07.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Predictive markers are factors that are associated with upfront response or resistance to a particular therapy. Predictive markers are important in oncology as tumors of the same tissue of origin vary widely in their response to most available systemic therapies. Currently recommended oncological predictive markers include both estrogen and progesterone receptors for identifying patients with breast cancers likely to benefit from hormone therapy. HER-2 for the identification of breast cancer patients likely to benefit from trastuzumab, specific K-RAS mutations for the identification of patients with advanced colorectal cancer unlikely to benefit from either cetuximab or panitumumab and specific EGFR mutations for selecting patients with advanced non-small-cell lung cancer for treatment with tyrosine kinase inhibitors such as gefitinib and erlotinib. The availability of predictive markers should increase drug efficacy and decrease toxicity, thus leading to a more personalized approach to cancer treatment. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:151 / 159
页数:9
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